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HRID 583482作成日:2026年10月26日

N-Trimethylsilyl-N-methylacetamide → N-[(4-sulfamoylphenyl)methyl]-2-[[2-[(4-sulfamoylphenyl)methylcarbamoyl]phenyl]disulfanyl]benzamide

https://huagongshe.com/reaction/583482

反応式

関与物質

役割名称HCID仕込み量
反応物N-Trimethylsilyl-N-methylacetamideHCID 81953—
反応物2,2'-Dithiodibenzoyl chlorideHCID 88164—
反応物4-(Aminomethyl)benzenesulfonamide hydrochloride hydrateHCID 21584567—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物N-[(4-sulfamoylphenyl)methyl]-2-[[2-[(4-sulfamoylphenyl)methylcarbamoyl]phenyl]disulfanyl]benzamideHCID 46536935.4%

反応手順

A slurry of 4-(aminomethyl)benzenesulfonamide hydrochloride hydrate (6.5 gf 29 mmol) in 100 mL pyridine was allowed to stir with N-methyl-N-(trimethylsilyl)acetamide (13.4 mL, 83.0 mmol) until a homogenous solution occurred. The solution was cooled to 0° C. to 5° C. and a solution of 2,2'-dithiobisbenzoyl chloride (4.0 g, 16.0 mmol) in 20 mL dichloromethane was added dropwise. The resulting solution was allowed to stir for 18 hours and the dichloromethane was removed in vacuo. The crude product was precipitated with the addition of water and the resulting solid was collected by filtration. The crude product was recrystallized from a mixture of dimethylformamide, ethanol, and water to yield 3.3 g of the title compound, mp 267-269° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05929114
出典データセットuspto-grants-1999_07
ORD IDord-5aad2cea920c49739b25da5c2dc544c4
出典メモuspto-grants-1999_07